Genetic Analysis of Oculocutaneous Albinism Type1A (OCA1A) in an Iranian Family

"nBackground: Oculocutaneous albinism type1 (OCA1) is characterized by the absence of melanin pigmentation. The muta­tion on TYR gene makes OCA1 as an autosomal recessive genetic disorder. In this study, we delineated the genetic analysis of an Iranian family with four members affected...

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Main Authors: H Pour-Jafari (Author), A Zamanian (Author), B Pour-Jafari (Author)
Format: Book
Published: Tehran University of Medical Sciences, 2010-03-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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